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Richard I. Grauch

Publications and source records attributed to Richard I. Grauch.

At least 19 recordsLinked to original sources
USGS2014

Contaminants from Cretaceous black shale: I. Natural weathering processes controlling contaminant cycling in Mancos Shale, southwestern United States, with emphasis on salinity and selenium

Soils derived from black shale can accumulate high concentrations of elements of environmental concern, especially in regions with semiarid to arid climates. One such region is the Colorado River basin in the southwestern United States where contaminants pose a threat to agriculture, municipal water supplies, endangered aquatic species, and water-quality commitments to Mexico. Exposures of Cretaceous Mancos Shale (MS) in the upper basin are a major contributor of salinity and selenium in the Colorado River. Here, we examine the roles of geology, climate, and alluviation on contaminant cycling (emphasis on salinity and Se) during weathering of MS in a Colorado River tributary watershed. Stage I (incipient weathering) began perhaps as long ago as 20 ka when lowering of groundwater resulted in oxidation of pyrite and organic matter. This process formed gypsum and soluble organic matter that persist in the unsaturated, weathered shale today. Enrichment of Se observed in laterally persistent ferric oxide layers likely is due to selenite adsorption onto the oxides that formed during fluctuating redox conditions at the water table. Stage II weathering (pedogenesis) is marked by a significant decrease in bulk density and increase in porosity as shale disaggregates to soil. Rainfall dissolves calcite and thenardite (Na 2 SO 4 ) at the surface, infiltrates to about 1 m, and precipitates gypsum during evaporation. Gypsum formation (estimated 390 kg m −2 ) enriches soil moisture in Na and residual SO 4 . Transpiration of this moisture to the surface or exposure of subsurface soil (slumping) produces more thenardite. Most Se remains in the soil as selenite adsorbed to ferric oxides, however, some oxidizes to selenate and, during wetter conditions is transported with soil moisture to depths below 3 m. Coupled with little rainfall, relatively insoluble gypsum, and the translocation of soluble Se downward, MS landscapes will be a significant nonpoint source of salinity and Se to the Colorado River well into the future. Other trace elements weathering from MS that are often of environmental concern include U and Mo, which mimic Se in their behavior; As, Co, Cr, Cu, Ni, and Pb, which show little redistribution; and Cd, Sb, V, and Zn, which accumulate in Stage I shale, but are lost to varying degrees from upper soil intervals. None of these trace elements have been reported previously as contaminants in the study area.

Colorado↗
USGS2014

Contaminants from Cretaceous black shale: II. Effect of geology, weathering, climate, and land use on salinity and selenium cycling, Mancos Shale landscapes, southwestern United States

The Cretaceous Mancos Shale (MS) is a known nonpoint source for a significant portion of the salinity and selenium (Se) loads in the Colorado River in the southwestern United States and northwestern corner of Mexico. These two contaminants pose a serious threat to rivers in these arid regions where water supplies are especially critical. Tuttle et al. (companion paper) investigates the cycling of contaminants in a Colorado River tributary watershed (Uncompahgre River, southwestern Colorado) where the MS weathers under natural conditions. This paper builds on those results and uses regional soil data in the same watershed to investigate the impact of MS geology, weathering intensity, land use, and climate on salt and Se storage in and flux from soils on the natural landscape, irrigated agriculture fields, areas undergoing urban development, and wetlands. The size of salinity and Se reservoirs in the MS soils is quantified. Flux calculations show that during modern weathering, natural landscapes cycle salt and Se; however, little of it is released for transport to the Uncompahgre River (10% of the annual salinity and 6% of the annual Se river loads). When irrigated, salinity and Se loads from the MS soil increase (26% and 57% of the river load, respectively), causing the river to be out of compliance with Federal and State Se standards. During 100 years of irrigation, seven times more Se has been removed from agricultural soil than what was lost from natural landscapes during the entire period of pedogenesis. Under more arid conditions, even less salt and Se are expected to be transported from the natural landscape. However, if wetter climates prevail, transport could increase dramatically due to storage of soluble phases in the non-irrigated soil. These results are critical input for water-resource and land-use managers who must decide whether or not the salinity and Se in a watershed can be managed, what sustainable mitigation strategies are possible, and what landscapes should be targeted. The broader implications include providing a reliable approach for quantifying nonpoint-source contamination from MS and other rock units elsewhere that weather under similar conditions and, together with results from our companion paper, address the complex interplay of geology, weathering, climate, and land use on contaminant cycling in the arid Southwest.

Colorado↗
USGS2012

Multiple age components in individual molybdenite grains

Re–Os geochronology of fractions composed of unsized, coarse, and fine molybdenite from a pod of unusual monazite–xenotime gneiss within a granulite facies paragneiss, Hudson Highlands, NY, yielded dates of 950.5 ± 2.5, 953.8 ± 2.6, and 941.2 ± 2.6 Ma, respectively. These dates are not recorded by co-existing zircon, monazite, or xenotime. SEM–BSE imagery of thin sections and separated grains reveals that most molybdenite grains are composed of core and rim plates that are approximately perpendicular. Rim material invaded cores, forming irregular contacts, probably reflecting dissolution/reprecipitation. EPMA and LA-ICP-MS analyses show that cores and rims have different trace element concentrations (for example, cores are relatively enriched in W). On the basis of inclusions of zircon with metamorphic overgrowths, we conclude that molybdenite cores and rims formed after high-grade regional metamorphism. The discovery of cores and rims in individual molybdenite grains is analogous to multi-component U-Pb geochronometers such as zircon, monazite, and titanite; thus, molybdenite should be carefully examined before dating to ensure that the requirement of age homogeneity is fulfilled.

New York↗
USGS2010

Chemistry of selected core samples, concentrate, tailings, and tailings pond waters: Pea Ridge iron (-lanthanide-gold) deposit, Washington County, Missouri

The Minerals at Risk and for Emerging Technologies Project of the U.S. Geological Survey (USGS) Mineral Resources Program is examining potential sources of lanthanide elements (rare earth elements) as part of its objective to provide up-to-date geologic information regarding mineral commodities likely to have increased demand in the near term. As part of the examination effort, a short visit was made to the Pea Ridge iron (-lanthanide-gold) deposit, Washington County, Missouri in October 2008. The deposit, currently owned by Wings Enterprises, Inc. of St. Louis, Missouri (Wings), contains concentrations of lanthanides that may be economic as a primary product or as a byproduct of iron ore production. This report tabulates the results of chemical analyses of the Pea Ridge samples and compares rare earth elements contents for world class lanthanide deposits with those of the Pea Ridge deposit. The data presented for the Pea Ridge deposit are preliminary and include some company data that have not been verified by the USGS or by the Missouri Department of Natural Resources, Division of Geology and Land Survey (DGLS), Geological Survey Program (MGS). The inclusion of company data is for comparative purposes only and does not imply an endorsement by either the USGS or MGS.

Missouri↗
USGS2010

U.S. Geological Survey Science for the Wyoming Landscape Conservation Initiative-2009 Annual Report

This is the second report produced by the U.S. Geological Survey (USGS) for the Wyoming Landscape Conservation Initiative (WLCI) to detail annual work activities. The first report described work activities for 2007 and 2008; this report covers work activities conducted in 2009. Important differences between the two reports are that (1) this report does not lump all the Effectiveness Monitoring activities together as last year's report did, which will allow WLCI partners and other readers to fully appreciate the scope and accomplishments of those activities, and (2) this report does not include a comprehensive appendix of the background details for each work activity. In 2009, there were 29 ongoing or completed activities, and there were 5 new work activities conducted under the 5 original major multi-disciplinary science and technical assistance activities: (1) Baseline Synthesis; (2) Targeted Monitoring and Research; (3) Data and Information Management; (4) Integration and Coordination; and (5) Decisionmaking and Evaluation. New work included (1) developing a soil-quality index, (2) developing methods for assessing levels of and relationships between mercury and soil organic matter, and (3) ascertaining element source, mobility, and fate. Additionally, (4) remotely sensed imagery was used to assess vegetation as an indicator of soil condition and geology, and (5) an Integrated Assessment (IA) was initiated to synthesize what has been learned about WLCI systems to date, and to develop associated decision tools, maps, and a comprehensive report.

Open-File Report↗
USGS2009

U.S. Geological Survey Science for the Wyoming Landscape Conservation Initiative - 2008 Annual Report

The Wyoming Landscape Conservation Initiative (WLCI) was launched in 2007 in response to concerns about threats to the State's world class wildlife resources, especially the threat posed by rapidly increasing energy development in southwest Wyoming. The overriding purpose of the WLCI is to assess and enhance aquatic and terrestrial habitats at a landscape scale, while facilitating responsible energy and other types of development. The WLCI includes partners from Federal, State, and local agencies, with participation from public and private entities, industry, and landowners. As a principal WLCI partner, the U.S. Geological Survey (USGS) provides multidisciplinary scientific and technical support to inform decisionmaking in the WLCI. To address WLCI management needs, USGS has designed and implemented five integrated work activities: (1) Baseline Synthesis, (2) Targeted Monitoring and Research, (3) Integration and Coordination, (4) Data and Information Management, and (5) Decisionmaking and Evaluation. Ongoing information management of data and products acquired or generated through the integrated work activities will ensure that crucial scientific information is available to partners and stakeholders in a readily accessible and useable format for decisionmaking and evaluation. Significant progress towards WLCI goals has been achieved in many Science and Technical Assistance tasks of the work activities. Available data were identified, acquired, compiled, and integrated into a comprehensive database for use by WLCI partners and to support USGS science activities. A Web-based platform for sharing these data and products has been developed and is already in use. Numerous map products have been completed and made available to WLCI partners, and other products are in progress. Initial conceptual, habitat, and climate change models have been developed or refined. Monitoring designs for terrestrial and aquatic indicators have been completed, pilot data have been collected for terrestrial indicators, and evaluations of alternative monitoring designs are underway. Initial models and map products have been developed for assessing vegetation, surface disturbance, oil and gas resources, mineral resources, surficial geology, invasive species, aspen treatments, ungulate migration corridors, greater sage-grouse (Centrocercus urophasianus), pygmy rabbits (Brachylagus idahoensis), and songbirds, and data were collected or compiled to validate and refine the models. Coordination and collaboration among partners has led to the production of several documents addressing WLCI objectives, strategies, and guiding principles, and has facilitated implementation of on-the-ground habitat treatments.

Open-File Report↗
USGS2009

Salinization of the upper Colorado River - Fingerprinting geologic salt sources

Salt in the upper Colorado River is of concern for a number of political and socioeconomic reasons. Salinity limits in the 1974 U.S. agreement with Mexico require the United States to deliver Colorado River water of a particular quality to the border. Irrigation of crops, protection of wildlife habitat, and treatment for municipal water along the course of the river also place restrictions on the river's salt content. Most of the salt in the upper Colorado River at Cisco, Utah, comes from interactions of water with rock formations, their derived soil, and alluvium. Half of the salt comes from the Mancos Shale and the Eagle Valley Evaporite. Anthropogenic activities in the river basin (for example, mining, farming, petroleum exploration, and urban development) can greatly accelerate the release of constituents from these geologic materials, thus increasing the salt load of nearby streams and rivers. Evaporative concentration further concentrates these salts in several watersheds where agricultural land is extensively irrigated. Sulfur and oxygen isotopes of sulfate show the greatest promise for fingerprinting the geologic sources of salts to the upper Colorado River and its major tributaries and estimating the relative contribution from each geologic formation. Knowing the salt source, its contribution, and whether the salt is released during natural weathering or during anthropogenic activities, such as irrigation and urban development, will facilitate efforts to lower the salt content of the upper Colorado River.

Colorado↗
USGS2007

Results of chemical analyses of soil, shale, and soil/shale extract from the Mancos Shale formation in the Gunnison Gorge National Conservation Area, southwestern Colorado, and at Hanksville, Utah

Results of chemical and some isotopic analyses of soil, shale, and water extracts collected from the surface, trenches, and pits in the Mancos Shale are presented in this report. Most data are for sites on the Gunnison Gorge National Conservation Area (GGNCA) in southwestern Colorado. For comparison, data from a few sites from the Mancos landscape near Hanksville, Utah, are included. Twelve trenches were dug on the GGNCA from which 258 samples for whole-rock (total) analyses and 187 samples for saturation paste extracts were collected. Sixteen of the extract samples were duplicated and subjected to a 1:5 water extraction for comparison. A regional soil survey across the Mancos landscape on the GGNCA generated 253 samples for whole-rock analyses and saturation paste extractions. Seventeen gypsum samples were collected on the GGNCA for sulfur and oxygen isotopic analysis. Sixteen samples were collected from shallow pits in the Mancos Shale near Hanksville, Utah.

Colorado, Utah↗
USGS2007

Petrographic Descriptions of Selected Rock Specimens From the Meade Peak Phosphatic Shale Member, Phosphoria Formation (Permian), Southeastern Idaho

Based on petrographic observations of 135 thin sections, rocks in the Meade Peak Phosphatic Shale Member of the Permian Phosphoria Formation in southeastern Idaho can be placed into one of four major lithofacies: organic claystone, muddy siltstone, peloidal phosphorite, and dolomitized calclithite-in order of decreasing abundance. Organic claystones are the most common lithofacies in the Meade Peak. Many of these rocks contain sufficient amounts of silt to make silty, organic claystones a common subtype. Organic claystones commonly contain crystals of muscovite and bioclasts as accessory components, and they are typically parallel laminated. Muddy siltstones are composed primarily of quartz silt, but some feldspar and rare carbonate silt are also present; some rocks are parallel laminated. Phosphate peloids are composed of varying amounts of opaque, complex, and translucent material, and observed internal structures are classified as simple, banded, cored, zoned, oolitic, nucleated, and polynucleated. Opaque, complex, and translucent peloids form the framework grains of three peloidal phosphorite rocks: wackestone phosphorite, packstone phosphorite, and grainstone phosphorite. Wackestone phosphorite is phosphatic-mud supported and contains more than 10 percent peloids; it is the most common type of phosphorite. Packstone phosphorite is peloid supported and contains interstitial phosphatic mud; it is also a common type. Grainstone phosphorite is peloid supported but lacks phosphatic mud; it is the least common type. Dolomitized calclithites contain three types of carbonate grains: macrocrystalline, microcrystalline, and crystalline with a microcrystalline nuclei-in order of decreasing abundance. Based on chemical staining and X-ray diffraction analyses, most of the carbonate is dolomite. Sufficient amounts of quartz silt or muddy material allow some rocks to be called silty dolomitized calclithite or muddy dolomitized calclithite, respectively. Sedimentary structures are absent except in some muddy dolomitized calclithites. Organic claystones, muddy siltstones, and dolomitized calclithites are detrital deposits. Many rocks in the Meade Peak contain calcite and apatite as fracture fillings and vug linings. As expected, peloidal phosphorites are most common in ore zones, and detrital rocks are most common in waste zones. Mine-specific marker beds are mostly composed of dolomitized calclithite.

Scientific Investigations Report↗
USGS2004

Chapter 8 Petrogenesis and mineralogic residence of selected elements in the meade peak phosphatic shale member of the permian phosphoria formation, Southeast Idaho

The Meade Peak Phosphatic Shale Member of the Permian Phosphoria Formation hosts the ore mined by the phosphate industry of southeast Idaho. It also hosts environmentally sensitive elements (ESE) such as Se, As, Hg, Ni, Cd, Zn, and Cr. Primary chemistry, elemental distribution patterns, and mineralogy within the Meade Peak were modified by element migration and possibly the introduction of elements. Fluids moved within the Meade Peak throughout its history, although the passage of fluids was highly variable in space and time, resulting in small domains of different rock chemistry and different mineralogy. Timing of major events affecting the Meade Peak and mineral habit are used to differentiate among detrital, diagenetic, epigenetic, and supergene mineral assemblages. Cross-cutting relationships among minerals are too rare to provide much paragenetic infor- mation. Carbonate fluorapatite (CFA) occurs in several forms, but dominantly as pelloids, some of which may have formed in situ during diagenesis. The other volumetrically signifi- cant form of CFA is interstitial cement that formed during diagenesis. Beginning during diagenesis and continuing intermittently, multiple generations of carbonate (dolomite and calcite) formed overgrowths and texturally complex carbonate cements. Movement and precipitation of silica followed a similar pattern. The ammonium feldspar buddingtonite, which generally rims orthoclase, also formed during diagenesis. Bacteria apparently played a significant role during diagenesis as well as during supergene processes, resulting in extreme fractionation of S isotopes and the possible bacterially mediated formation of minerals such as glauconite and sphalerite. Catagenesis, apparently culminating in oil generation, was the last significant diagenetic change. Thrusting accompanied by fluid (oil and brine) migration began during catagenesis in the Late Jurassic or Cretaceous and continued into the early Eocene. Fluorite ± carbonate ± barite± bitumen veins formed as a result of brittle deformation and accompanying fluid movement. This fracturing event may have been associated with a period of extension and normal faulting (Neogene to Holocene). Passage of the Yellowstone hot spot to the north of the area during the Neogene is marked by silicic domes and basaltic flows. The enrichment of Hg in fracture coatings might be the result of deposition from warm fluids associated with the emplacement of the silicic domes or a generally elevated, regional thermal gradient associated with the volcanism. Many of the fracture systems are still open and continue to provide fluid pathways that are the primary depositional sites for a wide variety of supergene minerals (such as Se, efflorescent salts) and element associations (such as Hg, Cd-S, Fe-Cr-O) in which many of the ESE are concentrated. Native Se is the most commonly identified host of Se in the studied samples. The largest concentration of Se occurs in open-fracture systems that cross-cut waste rock and ore units. The age(s) of native Se formation is not known; how- ever, the latest period of Se mobility is the present. Direct measurement of efflorescent “salts” forming on new mine faces indicate that several ESE, including both Se and Zn, are concentrated on the faces soon after they are exposed. Zinc is present as hydrous sulfates, but the residence of Se in these “salts” is unknown.

Idaho↗
USGS2004

Weathering of the meade peak phosphatic shale member, phosphoria formation: Observations based on uranium and its decay products

Variably weathered outcrop samples of the Meade Peak Phosphatic Shale Member of the Phosphoria Formation have 5-10% of the contained uranium (U) in a form readily extractable by 0.1 M sodium bicarbonate. Fission track radiography of outcrop samples and other less-weathered channel and core samples indicate that this mobile fraction of U is likely hosted by organic matter, secondary iron oxides and clay minerals, trace uraninite, and very fine-grained apatite cement. During weathering, this extractable U fraction is especially susceptible to redistribution, which produces small but measurable departures (1-15%) from radioactive (secular) equilibrium in the 238 U decay-series. The most weath- ered samples show the strongest isotopic evidence for redistribution of U during the last 350 ka, but sequestration of U by alteration products limits open-system losses of U at the whole-rock scale. In less-weathered samples, isotopic evidence for minor U loss (or gain) over longer time periods (1 Ma) is consistent with relatively non-aggressive attack of phosphatic rock during weathering. Comparative extractability of selenium (Se) suggests that a larger fraction of Se (19%) is readily available for mobilization during the earliest stages of weathering.

Book chapter↗
USGS1979

New geologic, ground magnetic, E-mode VLF, and radiometric surveys at Phillips Mine-Camp Smith uranium prospect, Westchester and Putnam Counties, New York

This report updates U.S. Geological Survey Open-File Report 77-780 by including new field data taken in July 1978. A revised geologic map is included, as are new geophysical data from an approximately 0.3-km by 0.5-km area just northeast of and adjoining the area surveyed earlier. The pattern which had been observed to the southwest of spatially coincident radiometric highs, magnetic highs, and resistivity lows deteriorates to the northeast: there the radiometric highs fall on magnetic lows and the correlation with resistivity lows disappears.

New York↗
USGS1978

Geology of the uranium prospect at Camp Smith, New York, with a new model for the formation of uranium deposits in metamorphosed submarine volcanogenic rocks

Uraninite of Precambrian age occurs locally in and around a massive sulfide deposit at Camp Smith, Westchester and Putnam Counties, New York. The host rocks are believed to be part of a sequence of marine sediments and submarine volcanogenic rocks that were metamorphosed to leucogneisses, amphibolites, and amphoholite gneisses in the granulite facies. Ore grade concentrations of uraninite occur (1) in the outer Cu-Ni-bearing zone of the sulfide body; (2) in magnetite-rich and scapolite-rich layers within amphibolite gneiss; and (3) in amphibole-quartz-feldspar + pyroxene pegmatites. The uranium-rich horizons are generally near the contact between rocks of keratophyre and spilite affinities. It is suggested that the iron oxide, uranium-rich, and sulfide-rich horizons and their host rocks were originally deposited in the distal, volcanogenic, massive sulfide environment.

New York↗